Evidence map›Paper›PMID 31002441›Full record

ArticleDrug development research2019

Further modifications of 1H-pyrrolo[2,3-b]pyridine derivatives as inhibitors of human neutrophil elastase.

Maria P Giovannoni, Niccolò Cantini, Letizia Crocetti, Gabriella Guerrini, Antonella Iacovone, Igor A Schepetkin, Claudia Vergelli, Andrei I Khlebnikov, Mark T Quinn

Open access · greenAbstract read
In one paragraph

Article in Drug development research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Imidazo[2,1-Antibiotics (Basel, Switzerland) · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 3 countries.

Maria P GiovannoniNEUROFARBA, Pharmaceutical and Nutraceutical Section, University of Florence, Sesto Fiorentino, Italy.
Niccolò CantiniNEUROFARBA, Pharmaceutical and Nutraceutical Section, University of Florence, Sesto Fiorentino, Italy.
Letizia CrocettiNEUROFARBA, Pharmaceutical and Nutraceutical Section, University of Florence, Sesto Fiorentino, Italy.ORCID 0000-0003-3473-2683
Gabriella GuerriniNEUROFARBA, Pharmaceutical and Nutraceutical Section, University of Florence, Sesto Fiorentino, Italy.
Antonella IacovoneNEUROFARBA, Pharmaceutical and Nutraceutical Section, University of Florence, Sesto Fiorentino, Italy.
Igor A SchepetkinDepartment of Microbiology and Immunology, Montana State University, Bozeman, Montana.
Claudia VergelliNEUROFARBA, Pharmaceutical and Nutraceutical Section, University of Florence, Sesto Fiorentino, Italy.
Andrei I KhlebnikovKizhner Research Center, Tomsk Polytechnic University, Tomsk, Russia.
Mark T QuinnDepartment of Microbiology and Immunology, Montana State University, Bozeman, Montana.
University of Florence · ITMontana State University · USAltai State University · RU

Funding

Pilot Grants ProgramP30GM110732 · NIGMS · MONTANA STATE UNIVERSITY - BOZEMAN · PI QUINN, MARK T · 2014 to 2018
$5.4M
NIGMS NIH HHS P30 GM110732
6 · The paper itself

Abstract

Human neutrophil elastase (HNE) is a potent protease that plays an important physiological role in many processes and is considered to be a multifunctional enzyme. HNE is also involved in a variety of pathologies affecting the respiratory system. Thus, compounds able to inhibit HNE proteolytic activity could represent effective therapeutics. We present here a new series of pyrrolo[2,3-b]pyridine derivatives of our previously reported potent HNE inhibitors. Our results show that position 2 of the pyrrolo[2,3-b]pyridine scaffold must be unsubstituted, and modifications of this position resulted in loss of HNE inhibitory activity. Conversely, the introduction of certain substituents at position 5 was tolerated, with retention of HNE inhibitory activity (IC

Indexed as

Enzyme InhibitorsHumansLeukocyte ElastaseModels, MolecularMolecular Docking SimulationMolecular StructurePyridinesStructure-Activity RelationshipELANE protein, humanEnzyme InhibitorsLeukocyte ElastasePyridineshuman neutrophil elastase inhibitorsmolecular dockingpyrrolo[2,3-b]pyridine

Identifiers

PMID31002441
PMCPMC6687522
OpenAlexW2939515251

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.